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Open Access research that solves space system engineering problems...

Strathprints makes available scholarly Open Access content by scholars in the Departments of Mechanical & Aerospace Engineering, Electronic & Electrical Engineering, and Design, Manufacturing & Engineering Management -- all active in the areas of space systems engineering, space mechatronics, aerospace and astronautical engineering. This spans a wide variety of topics such as nano-satellites, self-assembling spacecraft, robotics, flightpath mechanics, orbital dynamics, trajectory design and optimization, autonomous navigation and planning -- and with almost all research outputs openly available through Strathprints.

Explore the Open Access research of the Mechanical & Aerospace Engineering, Electronic & Electrical Engineering, and Design, Manufacturing & Engineering Management. Or explore all of Strathclyde's Open Access research...

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Number of items: 4.

Martin, Antony P. and Downing, Jennifer and Collins, Brendan and Godman, Brian and Alfirevic, Ana and Greenhalgh, Karen Lynn and Pirmohamed, Munir (2021) Examining the uptake of predictive BRCA testing in the UK; findings and implications. European Journal of Human Genetics, 29. pp. 699-708. ISSN 1018-4813

Martin, Antony P. and Pedra, Gabriel and Downing, Jennifer and Collins, Brendan and Godman, Brian and Alfirevic, Ana and Pirmohamed, Munir and Greenhalgh, Kathryn (2019) Trends in BRCA testing and socioeconomic deprivation. European Journal of Human Genetics, 27 (9). pp. 1351-1360. ISSN 1018-4813

Simpson, Nuala H and Ceroni, Fabiola and Reader, Rose H and Covill, Laura E and Knight, Julian C and Hennessy, Elizabeth R and Bolton, Patrick F and Conti-Ramsden, Gina and O'Hare, Anne and Baird, Gillian and Fisher, Simon E and Newbury, Dianne F and Nudel, R and Monaco, AP and Simonoff, E and Bolton, PF and Pickles, A and Slonims, V and Dworzynski, K and Everitt, A and Clark, A and Watson, J and Seckl, J and Cowie, H and Cohen, W and Nasir, J. and Bishop, DVM and Simkin, Z (2015) Genome-wide analysis identifies a role for common copy number variants in specific language impairment. European Journal of Human Genetics, 23 (10). pp. 1370-1377. ISSN 1018-4813

Knight, Helen M. and Maclean, Alan and Irfan, Muhammad and Naeem, Farooq and Cass, Stephen and Pickard, B.S. and Muir, Walter J. and Blackwood, D.H.R. (2008) Homozygosity mapping in a family presenting with schizophrenia, epilepsy and hearing impairment. European Journal of Human Genetics, 16 (6). pp. 750-758. ISSN 1018-4813

This list was generated on Fri Apr 16 10:39:39 2021 BST.